List of variants in gene DNAH11 reported by Mayo Clinic Laboratories, Mayo Clinic

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001277115.2(DNAH11):c.2500G>A (p.Val834Met)	rs368578923	0.00010
NM_001277115.2(DNAH11):c.10867A>G (p.Ile3623Val)	rs370443558	0.00008
NM_001277115.2(DNAH11):c.12569G>A (p.Gly4190Asp)	rs374787771	0.00008
NM_001277115.2(DNAH11):c.991G>A (p.Glu331Lys)	rs550602612	0.00006
NM_001277115.2(DNAH11):c.3685G>A (p.Ala1229Thr)

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